Congenital heart disease causes: Difference between revisions
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
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*[[Acrocephalopolysyndactyly type III]] | |||
*[[Alagille syndrome]] | |||
*[[Alcohol]] | |||
*[[Aortic stenosis]] | |||
*[[Assisted reproductive technology]] | |||
*[[Atrial septal defect]] | |||
*[[Atrioventricular septal defect]] | |||
*Barrow-Fitzsimmons syndrome | |||
*[[Benzodiazepines]] | |||
*Beuren-Williams syndrome | |||
*Cardiocranial syndrome | |||
*[[Cardiofaciocutaneous syndrome]] | |||
*[[CATCH 22 syndrome]] | |||
*[[CHARGE syndrome]] | |||
*Chromosome 8 recombinant syndrome | |||
*[[Costello syndrome]] | |||
*[[Coxsackie virus]] | |||
*[[Cytomegalovirus]] | |||
*[[DiGeorge's syndrome]] | |||
*[[Down syndrome]] | |||
*[[Drug abuse]] | |||
*[[Ebstein's anomaly]] | |||
*[[Edwards syndrome]] | |||
*[[Eisenmenger's syndrome]]<ref name="pmid24275297">{{cite journal| author=Opotowsky AR, Landzberg MJ, Beghetti M| title=The exceptional and far-flung manifestations of heart failure in Eisenmenger syndrome. | journal=Heart Fail Clin | year= 2014 | volume= 10 | issue= 1 | pages= 91-104 | pmid=24275297 | doi=10.1016/j.hfc.2013.09.005 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24275297 }} </ref> | |||
*[[Endocardial cushion defect]] | |||
*Faciocardiomelic syndrome | |||
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*Forney Robinson Pascoe syndrome | |||
*Gay-Feinmesser-Cohen syndrome | |||
*[[Gestational diabetes]] | |||
*Goossens-Devriendt syndrome | |||
*[[Herpes virus]] | |||
*Ho Kaufman Mcalister syndrome | |||
*Humerospinal dysostosis | |||
*Hurst-Hallam-Hockey syndrome | |||
*[[Hydantoin]] | |||
*[[Hypoplastic left heart syndrome]] | |||
*[[Ibuprofen]] | |||
*[[Isotretinoin]] | |||
*[[Leopard syndrome]] | |||
*[[Lissencephaly syndrome type 1]] | |||
*[[Lithium]] | |||
*[[Loeys-Dietz syndrome]] | |||
*Lymphedema-distichiasis syndrome <ref name="pmid12114478">{{cite journal| author=Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF et al.| title=Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. | journal=J Med Genet | year= 2002 | volume= 39 | issue= 7 | pages= 478-83 | pmid=12114478 | doi= | pmc=PMC1735188 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12114478 }} </ref> | |||
*[[Marfan syndrome]] | |||
*[[diabetes mellitus|Maternal diabetes mellitus]] | |||
*[[Mitral stenosis]] | |||
*[[Moyamoya disease]] | |||
*[[Neonatal lupus]] | |||
*[[Noonan syndrome]] | |||
*[[Organic solvents]] | |||
*[[Patent ductus arteriosus]] | |||
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*[[Pfeiffer syndrome|Pfeiffer syndrome type III]] | |||
*[[Phenylketonuria]] | |||
*[[Pulmonary atresia]] | |||
*[[Pulmonic stenosis]] | |||
*[[Retinoic acid]] | |||
*[[Rubella]] | |||
*[[Sakati syndrome]] | |||
*[[Systemic lupus erythematosus]] | |||
*[[Tetralogy of Fallot]] | |||
*[[Thalidomide]] | |||
*[[Total anomalous pulmonary venous connection]] | |||
*[[Transposition of the great vessels]] | |||
*[[Tricuspid atresia]] | |||
*[[Tricuspid stenosis]] | |||
*[[Trisomy 13]] | |||
*[[Trisomy 18]] | |||
*[[Trisomy 21]] | |||
*[[Truncus arteriosus]] | |||
*[[Turner syndrome]] | |||
*[[VACTERL association]] | |||
*[[Ventricular septal defect]] | |||
*[[Williams syndrome]] | |||
*[[Yorifuji Okuno syndrome]] | |||
*[[Zunich neuroectodermal syndrome]] | |||
*[[Zunich-Kaye syndrome]] | |||
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==References== | ==References== | ||
Revision as of 16:42, 5 November 2014
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Congenital heart disease Microchapters |
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Differentiating Congenital heart disease from other Disorders |
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Diagnosis |
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Treatment |
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Case Studies |
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Congenital heart disease causes On the Web |
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American Roentgen Ray Society Images of Congenital heart disease causes |
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Risk calculators and risk factors for Congenital heart disease causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Priyamvada Singh, MBBS [2] Ogheneochuko Ajari, MB.BS, MS [3] Assistant Editor-In-Chief: Kristin Feeney, B.S. [4]
Overview
Current knowledge regarding the causes of congenital heart disease is limited. Most research has been based on small studies (<1,000 patients). As is common with many congenital related conditions, there are gaps in knowledge regarding the causation of congenital heart disease. Congenital heart disease is multi-factorial in origin, with genetics and environmental factors both playing a role.
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
- Aortic stenosis
- Atrial septal defect[1]
- Coarctation of the aorta
- Down syndrome[2]
- Ebstein's anomaly
- Endocardial cushion defect
- Hypoplastic left heart syndrome
- Noonan syndrome[2]
- Patent ductus arteriosus
- Pulmonary atresia
- Pulmonic stenosis
- Tetralogy of Fallot
- Total anomalous pulmonary venous connection
- Transposition of the great vessels
- Turner syndrome
- Ventricular septal defect
Causes by Organ System
| Cardiovascular | No underlying causes |
| Chemical / poisoning | No underlying causes |
| Dermatologic | No underlying causes |
| Drug Side Effect | No underlying causes |
| Ear Nose Throat | No underlying causes |
| Endocrine | No underlying causes |
| Environmental | No underlying causes |
| Gastroenterologic | No underlying causes |
| Genetic | No underlying causes |
| Hematologic | No underlying causes |
| Iatrogenic | No underlying causes |
| Infectious Disease | No underlying causes |
| Musculoskeletal / Ortho | No underlying causes |
| Neurologic | No underlying causes |
| Nutritional / Metabolic | No underlying causes |
| Obstetric/Gynecologic | No underlying causes |
| Oncologic | No underlying causes |
| Opthalmologic | No underlying causes |
| Overdose / Toxicity | No underlying causes |
| Psychiatric | No underlying causes |
| Pulmonary | No underlying causes |
| Renal / Electrolyte | No underlying causes |
| Rheum / Immune / Allergy | No underlying causes |
| Sexual | No underlying causes |
| Trauma | No underlying causes |
| Urologic | No underlying causes |
| Dental | No underlying causes |
| Miscellaneous | No underlying causes |
Causes in Alphabetical Order
References
- ↑ Liu JJ, Fan LL, Chen JL, Tan ZP, Yang YF (2014). "A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect". J Zhejiang Univ Sci B. 15 (9): 830–7. doi:10.1631/jzus.B1400062. PMC 4162884. PMID 25183037.
- ↑ 2.0 2.1 Prendiville TW, Gauvreau K, Tworog-Dube E, Patkin L, Kucherlapati RS, Roberts AE; et al. (2014). "Cardiovascular disease in Noonan syndrome". Arch Dis Child. 99 (7): 629–34. doi:10.1136/archdischild-2013-305047. PMID 24534818.
- ↑ Opotowsky AR, Landzberg MJ, Beghetti M (2014). "The exceptional and far-flung manifestations of heart failure in Eisenmenger syndrome". Heart Fail Clin. 10 (1): 91–104. doi:10.1016/j.hfc.2013.09.005. PMID 24275297.
- ↑ Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF; et al. (2002). "Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24". J Med Genet. 39 (7): 478–83. PMC 1735188. PMID 12114478.